Classifications

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  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
  • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
  • C07D239/72—Quinazolines; Hydrogenated quinazolines
  • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
  • C07D239/94—Nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
  • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
  • C07D491/10—Spiro-condensed systems

Definitions

• EGFR EGFR activates tyrosine kinase activity and thereby triggers reactions that lead to cellular proliferation. Overexpression and overactivity of EGFR could result in uncontrolled cell division — a predisposition for cancer. See, e.g., Science, 2004, 304:1497-1500. Compounds that inhibit the overexpression and overactivity of EGFR are therefore potential candidates for treating cancer.
• This invention is based on the discovery that a number of quinazoline compounds inhibit the activity of EGFR.
• One aspect of this invention relates to compound of the following formula:
• each of Ri, R 2 , and R 5 independently, is H, halo, nitro, amino, cyano, hydroxy, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, alkoxy, alkylthio, alkylcarbonyl, carboxy, alkoxycarbonyl, carbonylamino, sulfonylamino, aminocarbonyl, or aminosulfonyl; one OfR 3 and R 4 is H, halo, nitro, amino, cyano, hydroxy, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, alkoxy, alkylthio, alkylcarbonyl, carboxy, alkoxycarbonyl, carbonylamino, sulfonylamino, aminocarbonyl, or aminosulfonyl; one OfR 3 and R 4 is
• each of R a , R b , and R c independently, is H, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl, or R b and R c , together with the nitrogen atom to which they are attached, form a 3-12 membered saturated, unsaturated, or aromatic ring containing 1-3 heteroatoms selected from N, O and S; and each of R d and R e , independently, is H, alkyl, alkenyl, or alkynyl; or R d and R e , together with the nitrogen to which they are attached, form a 3-12 membered saturated, unsaturated, or aromatic ring containing 1-3 heteroatoms selected from N, O, and S; and the other of R3 and R 4 is H, halo, nitro, amino, cyano, hydroxy, alkyl, alkenyl, alkynyl, aryl, cycloalky
• R 3 and R 4 is in which n is 1 and each of R a , R b , and R c , independently, is H, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl.
• R c in which n is 1 or 2; R a is H, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; and R b and R c , together with the nitrogen atom to which they are attached, form a 3-12 membered saturated, unsaturated, or aromatic ring containing 1-3 heteroatoms selected from N, O and S.
• R b and R c together with the nitrogen atom to which they are attached, form a bicyclic ring of the following formula: in which each of ni l , m 2 , m 3 , and Hi 4 , independently, is 0, 1, 2, or 3; A is N or CR; B is NR or CRR', each R and R', independently, being H, alkyl, or halo; and each OfR 1 , R 11 , R 111 , R 1V , R v , R V1 , R vu , and R V111 , independently, is H, alkyl, or halo. Still another subset of the compounds feature that one OfR 3 and R 4
• R a is H, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl.
• Still another subset of the compounds feature that one of R 3 and R 4 is
• R a is H, alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; and each of R d and R e , independently, is H, alkyl, alkenyl, or alkynyl; or R a is H, alkyl, alkenyl, or alkynyl; and R d and R e , together with the nitrogen to which they are attached, form a 3-12 membered saturated, unsaturated, or aromatic ring containing 1-3 heteroatoms selected from N, O, and S.
• alkyl herein refers to a straight or branched hydrocarbon, containing 1-10 carbon atoms.
• alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, /-propyl, n-butyl, /-butyl, and /-butyl.
• alkoxy refers to an -O-alkyl.
• alkenyl groups include, but are not limited to, vinyl, 2-propenyl, and 2-butenyl.
• alkynyl herein refers to a C 2-10 straight or branched hydrocarbon, containing one or more C ⁇ C triple bonds. Examples of alkynyl groups include, but are not limited to, ethynyl, 2-propynyl, and 2-butynyl.
• aryl refers to a 6-carbon monocyclic, 10-carbon bicyclic, 14- carbon tricyclic aromatic ring system wherein each ring may have 1 to 4 substituents.
• aryl groups include, but are not limited to, phenyl, naphthyl, and anthracenyl.
• cycloalkyl refers to a saturated and partially unsaturated cyclic hydrocarbon group having 3 to 12 carbons.
• examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.
• heteroaryl refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having one or more heteroatoms (such as O, N, or S).
• heteroaryl groups include pyridyl, furyl, imidazolyl, benzimidazolyl, pyrimidinyl, thienyl, quinolinyl, indolyl, and thiazolyl.
• heteroarylkyl refers to an alkyl group substituted with a heteroaryl group.
• heterocycloalkyl refers to a nonaromatic 3-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having one or more heteroatoms (such as O, N, or S).
• heterocycloalkyl groups include, but are not limited to, piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, and tetrahydrofuranyl.
• Heterocycloalkyl can be a saccharide ring, e.g., glucosyl.
• Alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and alkoxy mentioned herein include both substituted and unsubstituted moieties.
• substituents include, but are not limited to, halo, hydroxyl, amino, cyano, nitro, mercapto, alkoxycarbonyl, amido, carboxy, alkanesulfonyl, alkylcarbonyl, carbamido, carbamyl, carboxyl, thioureido, thiocyanato, sulfonamido, alkyl, alkenyl, alkynyl, alkyloxy, aryl, heteroaryl, cycloalkyl, heterocycloalkyl, in which alkyl, alkenyl, alkynyl, alkyloxy, aryl, heteroaryl cycloalkyl, and heterocycloalkyl may further substituted.
• the quinazoline compounds described above include their pharmaceutically acceptable salts, solvate, and prodrug, if applicable.
• Another aspect of this invention relates to a method of treating cancer.
• the method includes administering to a subject having cancer an effective amount of one or more of the quinazoline compounds of this invention.
• the cancer to be treated include, but are not limited to, lung cancer, head and neck cancer, colorectal cancer, pancreatic cancer, colon cancer, breast cancer, ovarian cancer, prostate cancer, stomach cancer, kidney cancer, liver cancer, brain cancer, bone cancer, and leukemia.
• compositions containing one or more of the quinazoline compounds described above and a pharmaceutically acceptable carrier for use in treating cancer and (2) use of one or more of the quinazoline compounds for the manufacture of a medicament for treating cancer.
• the quinazoline compounds of this invention can be synthesized from commercially available starting materials by methods well known in the art. For example, as shown in the scheme below, one can couple a suitable 4-chloro- quinazoline derivative with a benzene compound to obtain a compound of this invention.
• the compound thus obtained can be further modified at their peripheral positions to provide other compounds of this invention.
• Synthetic chemistry transformations useful in synthesizing desirable quinazoline compounds are described, for example, in R. Larock, Comprehensive Organic Transformations, VCH Publishers (1989); T.W. Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis, 3 rd Ed., John Wiley and Sons (1999); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995) and subsequent editions thereof.
• the compounds Before use, the compounds can be purified by column chromatography, high performance liquid chromatography, crystallization, or other suitable methods.
• the quinazoline compounds of this invention when contacting with EGFR, inhibit this receptor's activity.
• An effective amount of one or more of these compounds can be therefore used to treat cancers that are associated with over- expression and over-activity of EGFR.
• an effective amount refers to the amount of a quinazoline compound that is required to confer the intended effect in the subject. Effective amounts may vary, as recognized by those skilled in the art, depending on route of administration, excipient usage, and the possibility of co-usage with other agents.
• treating refers to administering one or more of the above-described quinazoline compounds to a subject that has cancer, or has a symptom of cancer, or has a predisposition toward cancer, with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve, or affect cancer, the symptoms of cancer, or the predisposition toward cancer.
• a composition having one or more of the quinazoline compounds of this invention can be administered orally, parenterally, by inhalation spray, or via an implanted reservoir.
• parenteral includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intraarterial, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.
• An oral composition can be any orally acceptable dosage form including, but not limited to, tablets, capsules, emulsions and aqueous suspensions, dispersions and solutions.
• Commonly used carriers for tablets include lactose and corn starch.
• Lubricating agents such as magnesium stearate, are also typically added to tablets.
• useful diluents include lactose and dried corn starch.
• the active ingredient can be suspended or dissolved in an oily phase combined with emulsifying or suspending agents. If desired, certain sweetening, flavoring, or coloring agents can be added.
• a sterile injectable composition e.g., aqueous or oleaginous suspension
• suitable dispersing or wetting agents such as, for example, Tween 80
• the sterile injectable preparation can also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3- butanediol.
• acceptable vehicles and solvents that can be employed are mannitol, water, Ringer's solution and isotonic sodium chloride solution.
• sterile, fixed oils are conventionally employed as a solvent or suspending medium (e.g., synthetic mono- or di-glycerides).
• Fatty acids such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions.
• oils such as olive oil or castor oil, especially in their polyoxyethylated versions.
• These oil solutions or suspensions can also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents.
• An inhalation composition can be prepared according to techniques well known in the art of pharmaceutical formulation and can be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.
• a topical composition can be formulated in form of oil, cream, lotion, ointment and the like.
• suitable carriers for the composition include vegetable or mineral oils, white petrolatum (white soft paraffin), branched chain fats or oils, animal fats and high molecular weight alcohols (greater than C 12).
• the preferred carriers are those in which the active ingredient is soluble.
• Emulsifiers, stabilizers, humectants and antioxidants may also be included as well as agents imparting color or fragrance, if desired.
• transdermal penetration enhancers may be employed in these topical formulations. Examples of such enhancers can be found in U.S. Patents 3,989,816 and 4,444,762.
• Creams are preferably formulated from a mixture of mineral oil, self-emulsifying beeswax and water in which mixture the active ingredient, dissolved in a small amount of an oil, such as almond oil, is admixed.
• An example of such a cream is one which includes about 40 parts water, about 20 parts beeswax, about 40 parts mineral oil and about 1 part almond oil.
• Ointments may be formulated by mixing a solution of the active ingredient in a vegetable oil, such as almond oil, with warm soft paraffin and allowing the mixture to cool.
• An example of such an ointment is one which includes about 30% by weight almond and about 70% by weight white soft paraffin.
• a carrier in a pharmaceutical composition must be "acceptable” in the sense that it is compatible with active ingredients of the formulation (and preferably, capable of stabilizing it) and not deleterious to the subject to be treated.
• solubilizing agents such as cyclodextrins (which form specific, more soluble complexes with one or more of active quinazoline compounds of the extract), can be utilized as pharmaceutical excipients for delivery of the active ingredients.
• examples of other carriers include colloidal silicon dioxide, magnesium stearate, cellulose, sodium lauryl sulfate, and D&C Yellow # 10.
• Suitable in vitro assays can be used to preliminarily evaluate the efficacy of the above-described quinazoline compounds in inhibiting the activity of EGFR.
• the compounds can further be examined for its efficacy in treating cancers by in vivo assays.
• the compounds can be administered to an animal (e.g., a mouse model) having cancer and its therapeutic effects are then accessed. Based on the results, an appropriate dosage range and administration route can also be determined.
• N4-(3-ethynylphenyl)-7-fluoroquinazoline-4,6-diamine (100 mg, 0.36 mmol) was dissolved into DMF (3 mL) containing pyridine (35 ⁇ L, 0.432 mmol). Phenyl chloro formate (46 ⁇ L, 0.36 mmol) was dropped into the mixture at room temperature and heated to 7O 0 C for 1 h to give phenyl 4-(3-ethynylphenylamino)-7- fluoroquinazolin-6-ylcarbamate. The obtained compound was used in the next step directly without purification.
• Example 85 Synthesis of l-(2-(dimethylamino)ethyl)-3- (4-(3- ethynylphenylamino)quinazolin-7-yl)-l-methylurea (Compound 85)
• the synthetic route to Compound 85 is shown below:
• N-(3-ethynylphenyl)-6-nitroquinazolin-4-amine (1.00 g, 3.45 mmol) and SnCl 2 -2H 2 O (3.10 g, 13.8 mmol) in ethyl acetate (35mL) were refiuxed for 2 h. After cooled to room temperature, the mixture was treated with 5% aqueous NaHCO 3 to adjust its pH to 9-10 and then subjected to extraction with EtOAc. The combined organic layers were washed with saturated brine and H 2 O, dried, and concentrated under reduced pressure to give 0.79 g (89%) of N4-(3-ethynylphenyl)quinazoline-4,6- diamine as a yellow solid. To a solution of N4-(3-ethynylphenyl)quinazoline-4,6-diamine (100 mg,
• Example 127 Synthesis of l-(4-(3-ethynylphenylamino)quinazolin -6-yl)- IH- imidazol-2(3H)-one
• Compound 127 was prepared in a manner similar to that described in Example 126.
• Example 128 Synthesis of l-(4-(3-ethynylphenylamino)quinazolin -6-yl)-3- (2- methoxy- ethyl)- lH-imidazol-2(3H)-one (Compound 128)
• Example 157 Synthesis of 3-(2-(dimethylamino)ethyl)-l- (4-(3- ethynylphenylamino)quinazolin-7-yl)-lH-imidazol-2(3H)-one (Compound 157)
• the Synthetic route to Compound 157 is shown below:
• N-(3-ethynylphenyl)-7-nitroquinazolin-4-amine (2.0 g, 6.89 mmol), SnCl 2 (5.0 g, 26.37 mmol), and ethyl acetate (50 mL) was refluxed for 3h.
• the mixture was subjected to extraction with ethyl acetate (20 mL).
• the combined organic layers were washed with brine (20 mLx2), dried over Na 2 SO 4 , and concentrated in vacuo to afford 1.6 g (86%) of N4-(3-ethynylphenyl)quinazoline-4,7-diamine as a yellow solid.
• N4-(3-ethynylphenyl)quinazoline-4,7-diamine 48mg, 0.18mmol
• phenyl carbonochloridate 25.2uL, 0.18mmol
• pyridine 32 ⁇ L
• DMF 2 mL
• Nl-(2,2- dimethoxyethyl)-N2,N2-dimethylethane-l,2-diamine 33.5 mg, 0.19 mmol.
• the mixture was stirred at 8O 0 C for 1 h and then p-toluenesulfonic acid (35.6 mg, 0.20 mmol) was added.
• Example 164 Synthesis of 3-(2-(diethylamino)ethyl)-l- (4-(3-ethynylphenylamino)- 7-fluoroquinazolin-6-yl)-lH-imidazol-2(3H)-one (Compound 164)
• the synthetic route to Compound 164 is shown below:
• 2-amino-4-fluorobenzoic acid (1.55 g, 10 mmol) was dissolved into formamide (5 mL) and stirred at 15O 0 C for 6 h. The mixture was cooled to room temperature with stirring. The precipitate was filtered out and washed with diethyl ether to give 1.3 g of 7-fluoroquinazolin-4-ol (78%).
• N4-(3-ethynylphenyl)-7-fluoroquinazoline-4,6-diamine 50 mg, 0.18 mmol was dissolved into DMF (2 mL) containing pyridine (17.5 ⁇ L, 0.21mmol). Phenyl chloroformate (23 ⁇ L, 0.18 mmol) was added to the mixture at room temperature and stirred at 7O 0 C for 1 h to give phenyl 4-(3-ethynylphenylamino) -7-fluoroquinazolin- 6-ylcarbamate.
• Nl-(2,2-diethoxyethyl)-N2,N2 -diethylethane-l,2-diamine (42mg, 0.18mmol) was added and stirred at 7O 0 C for 2.5 h. After cooled to room temperature, the reaction mixture was diluted with ethyl acetate and washed with water. The organic layer was concentrated and purified with a silica column to give 45 mg (70%) of l-(2,2-diethoxyethyl)-l-(2-(diethylamino) ethyl)-3-(4-(3- ethynylphenylamino)-7-fluoroquinazolin-6-yl)urea.
• Example 165 Synthesis of 3-(2-(diethylamino)ethyl)-l-(4- (3-ethynylphenylamino)- 7-methoxyquinazolin-6-yl)-lH-imidazol-2(3H)-one (Compound 165)
• the synthetic route to Compound 165 is shown below:
• Example 171 Inhibition of EGFR activity
• A431 cells (human epidermoid carcinoma) were seeded in DMEM at 2.5xlO 4 cells/well in 96-well plates and incubated overnight. The DMEM medium was discarded and the plates were washed with 200 ⁇ L of serum- free DMEM medium. After the medium was discarded, 90 ⁇ L serum- free DMEM medium was added to each well. The plates were incubated again overnight.
• Each test compound was dissolved in DMSO-containing (5%) FBS-free DMEM to prepare a series of solutions at the concentrations of 10, 3.3, 1.1, 0.37, 0.12, 0.04, 0.013, and 0.004 ⁇ M. Solutions of compounds at various concentrations were added to wells (10 ⁇ L/well) except controls. The plates were incubated under 5% CO 2 at 37 0 C for 60 min. 10 ⁇ L of 200 ng/ml EGF (Biosource, PHG0064) was added to each of the compound-treated wells and some of the controls, followed by incubation under 5% CO 2 at 37 0 C again for 45 min.
• EGF Biosource, PHG0064
• cell lysis buffer containing 50 mM Tris-Cl (pH 8.0), 0.5 M NaCl and 0.2 mM EDTA, 0.1% Triton X-100, and protease inhibitors (1 ⁇ g/ml aprotinin, 0.75 ⁇ g/ml leupeptin, 1 ⁇ g/ml pepstatin, 1 mM DTT, 500 ⁇ M sodium vanadate, and 1 mM PMSF). Note that the protease inhibitors were added immediately before use. The cell lysate was kept at -8O 0 C overnight
• the blocking buffer was discarded and the plate was washed with 200 ⁇ L of DELFIA wash buffer (PBS buffer containing 0.05% Tween-20) 3 times.
• 80 ⁇ L of sample diluent (20 mM Tris-Cl/pH7.3, 150 mM NaCl, 0.1% BSA, and 0.05% Tween- 20) and 20 ⁇ L of the above-obtained cell lysate were then added to each well. Incubation was continued at 25 0 C for 1 h with gentle shaking.
• the plate was washed again with 200 ⁇ L of DELFIA wash buffer 3 times.
• 100 ⁇ L of 0.5 ⁇ g/ml Eu-PT66 antibody (Perkin Elmer, AD0040) in DELFIA assay buffer (Perkin Elmer, 1244-106) was added and incubated at 25 0 C for 1 h with gentle shaking.
• 100 ⁇ L of DELFIA enhancement (Perkin Elmer, 4001-0010) was added. The incubation was continued at 25 0 C for 30 min with gentle shaking.
• Inhibition (%) 100 X 100% signal of EGF well - signal of cell well
• signal of compound well represents the fluorescence detected from the well which contained cells, a test compound, and EGF
• signal of cell well represents the fluorescence detected from the well which contained cells, but not a test compound and EGF
• signal of EGF well represents the fluorescence detected from the well which contained cells and EGF, but not a test compound

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  • 2009-06-30 KR KR1020107025451A patent/KR101664503B1/ko active IP Right Grant
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  • 2009-06-30 EP EP09774296.9A patent/EP2318378B1/en active Active
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  • 2009-06-30 RU RU2011103207/04A patent/RU2505534C2/ru active
  • 2009-06-30 WO PCT/US2009/049182 patent/WO2010002845A2/en active Application Filing
  • 2009-06-30 PT PT97742969T patent/PT2318378E/pt unknown
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